Mechanism and Control of Meiotic DNA Double-Strand Break Formation in S. cerevisiae
Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tig...
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Published in | Frontiers in cell and developmental biology Vol. 9; p. 642737 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
02.03.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tightly regulated to minimize potentially dangerous consequences for genomic integrity. In
, nine proteins participate with Spo11 in DSB formation, but their molecular functions have been challenging to define. Here, we describe our current view of the mechanism of meiotic DSB formation based on recent advances in the characterization of the structure and function of DSB proteins and discuss regulatory pathways in the light of recent models. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Reviewed by: Bernard De Massy, Université de Montpellier, France; Valérie Borde, Centre National de la Recherche Scientifique (CNRS), France This article was submitted to Cell Growth and Division, a section of the journal Frontiers in Cell and Developmental Biology Edited by: Akira Shinohara, Osaka University, Japan |
ISSN: | 2296-634X 2296-634X |
DOI: | 10.3389/fcell.2021.642737 |